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41498-06-0

5-BROMO-1-NAPHTHALDEHYDE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 41498-06-0 Structure

  • Basic information

    1. Product Name: 5-BROMO-1-NAPHTHALDEHYDE
    2. Synonyms: 5-BROMO-1-NAPHTHALDEHYDE;5-bromonaphthalene-1-carbaldehyde
    3. CAS NO:41498-06-0
    4. Molecular Formula: C11H7BrO
    5. Molecular Weight: 235.08
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 41498-06-0.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 5-BROMO-1-NAPHTHALDEHYDE(CAS DataBase Reference)
    10. NIST Chemistry Reference: 5-BROMO-1-NAPHTHALDEHYDE(41498-06-0)
    11. EPA Substance Registry System: 5-BROMO-1-NAPHTHALDEHYDE(41498-06-0)

  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 41498-06-0(Hazardous Substances Data)

41498-06-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 41498-06-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,1,4,9 and 8 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 41498-06:
(7*4)+(6*1)+(5*4)+(4*9)+(3*8)+(2*0)+(1*6)=120
120 % 10 = 0
So 41498-06-0 is a valid CAS Registry Number.

41498-06-0Relevant articles and documents

Palladium-Catalyzed Regiospecific peri- And ortho-C-H Oxygenations of Polyaromatic Rings Mediated by Tunable Directing Groups

Hu, Lihong,Jiang, Jing,Lin, Yaoyu,Ma, Congzhe,Song, Wanbin,Yuan, Dandan,Zhang, Yinan

supporting information, p. 279 - 284 (2021/01/13)

An efficient divergent approach of Pd-catalyzed C-H oxygenation of polyaromatic rings is described. Reversible directing groups enable regiospecific peri- and ortho-oxygenation to readily access a wide array of polyaromatic phenols without pre- and postmanipulation of directing groups. The systematic mechanistic investigation, including deuterium-labeling experiments, palladacycle trapping, and DFT calculations, reveals that the tunable ligand-assisted C-H bond cleavage played a crucial role during the reaction process.

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